Webinar – How to Ensure EUDAMED Compliance for Legacy Devices | Ackomas
The countdown is on: starting January 2026, all medical devices must be registered in EUDAMED. For Legacy Devices—those still certified under MDD/IVDD—this creates a strategic and operational compliance challenge. In 30 minutes, discover how to: – Identify which devices need registration – Choose the correct coding (Basic UDI-DI, UDI-DI…) – Anticipate workload and avoid non-compliance risks – Use automation to simplify EUDAMED submission Join experts from Ackomas and Efor for an actionable session to secure your compliance plan for 2025.
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Speakers
Hoegl Katharina
Florence Trépant
Jean-Philippe Joubert
Key Takeaways from the Webinar
Join our webinars to explore the latest regulatory compliance strategies in the medical device industry. Our experts provide practical solutions and answer your questions live.
Understand the Definition of Legacy Devices
Legacy devices are those certified under previous directives (MDD/IVDD) and placed on the market after MDR/IVDR dates. They benefit from a transition period—but require strict compliance conditions, including EUDAMED registration.
EUDAMED Registration Is Mandatory
By July 2026, all eligible legacy devices must be registered in EUDAMED, unless a corresponding MDR/IVDR device already exists. Failing to act could block market access.
Ackomas Simplifies Compliance
The Ackomas platform enables automated, secure, and traceable registration of legacy devices, transforming a complex process into a strategic advantage.
Act Early to Avoid Resource Bottlenecks
The closer to the deadline, the harder it becomes to access support and system availability. Starting now secures both time and quality.
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